Product Recalls in New Hampshire
Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,053 recalls have been distributed to New Hampshire in the last 12 months.
Showing 11921–11940 of 49,311 recalls
Recalled Item: Marketside Gouda Bacon Green Chile Dip Recalled by Morski Brands, Inc. Due...
The Issue: Foreign object (metal).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 13 OUNCE NATURAL CREAMY PEANUT BUTTER SQUEEZE POUCH Recalled by The JM...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 1.5 oz and 31.25 gram CREAMY PEANUT BUTTER TO GO packaged in 3 Recalled...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 340 GRAM CREAMY PEANUT BUTTER MEXICO Recalled by The JM Smucker Company...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF NATURAL CRUNCHY PEANUT BUTTER packaged in 16oz and 40oz Recalled by The...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System...
The Issue: Potential for stent dislodgement and associated failures related to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Item Number: 800774001 Recalled by ROi CPS LLC Due to A nonsterile...
The Issue: A nonsterile component was packaged in a sterile convenience kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis) Recalled by Agilent...
The Issue: Label provided for substrate vail contained incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...
The Issue: Complaints relating to urine output measurement accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension LTNI -In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 Recalled by...
The Issue: There is a potential for sporadic incidents of positive and negative biases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CATHCART FRACTURE HEAD HIP BALL Recalled by DePuy Orthopaedics, Inc....
The Issue: The Cathcart Ball has an inherent +5mm offset which is not currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension CTNI-In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine Hydrochloride Injection Recalled by Nephron Sterile Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprostadil Injection USP 500 mcg/mL Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Nephron Sterile Compounding Center LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Strides Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.